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CasNo: 3972-65-4
Molecular Formula: C10H13Br
Appearance: clear colorless to slightly yellow liquid
Trihalide salts were found to efficientl...
Methyl groups are ubiquitous in biologic...
Despite significant progress in aliphati...
Regioselective halogenation of arenes an...
(P(o-tol)3)2Pd2(C6H4tBu-4)2Br2
tri-tert-butyl phosphine
bis(tri-t-butylphosphine)palladium(0)
1-bromo-4-tert-butylbenzene
| Conditions | Yield |
|---|---|
|
In
benzene-d6;
byproducts: P(o-tol)3, biaryl, arene; in C6D6 soln. at 70°C; K(eq) = 3.3(6)E-4;
|
75% |
tert-butylbenzene
1-bromo-4-tert-butylbenzene
| Conditions | Yield |
|---|---|
|
With
bromine; iodine;
at 0 ℃;
|
100% |
|
With
carbon dioxide; bromine;
at 40 ℃;
for 2h;
under 187519 Torr;
Supercritical conditions;
Green chemistry;
|
100% |
|
With
benzyltrimethylazanium tribroman-2-uide; zinc(II) chloride;
In
acetic acid;
at 70 ℃;
for 2h;
|
95% |
|
With
bromine fluoride;
In
ethanol; chloroform;
at -78 ℃;
for 0.0833333h;
|
89% |
|
With
thallium (III) oxide; trifluoroacetic acid; potassium bromide;
at 20 ℃;
for 25h;
|
86% |
|
With
Li2MnO3; bromine; oxygen;
at 80 ℃;
for 3h;
under 760.051 Torr;
Photolysis;
|
86% |
|
With
bromine; iron;
In
tetrachloromethane;
at 0 ℃;
for 1h;
|
84% |
|
With
bromine;
In
dichloromethane;
at 0 ℃;
Inert atmosphere;
|
80% |
|
With
bromine; iron;
In
dichloromethane;
at 5 - 20 ℃;
for 24h;
|
71% |
|
With
styrene-4-vinyl(N-alkylpyridinium bromide);
In
water; acetic acid;
at 85 ℃;
for 5h;
|
59% |
|
With
bromine;
Sonnenlicht;
|
|
|
With
bromine; iron;
|
|
|
With
iodine;
durch Bromierung;
|
|
|
With
iron;
durch Bromierung;
|
|
|
With
bromine; iron;
|
|
|
With
bromine;
|
|
|
With
bromine; iodine; iron;
|
|
|
With
bromine; acetic anhydride; zinc(II) chloride;
In
acetic acid;
|
|
|
With
bromine; iron;
|
|
|
With
pyridine; bromine;
|
|
|
With
sodium metabisulfite; bromine;
Irradiation;
|
|
|
With
bromine fluoride; ethanol;
Yield given. Multistep reaction;
1.) CFCl3, -75 deg C; 2.) CHCl3, -75 deg C, 5-15 min;
|
|
|
With
bromine;
ZnBr2 on silica (100 Angstroem);
In
hexane;
at 25 ℃;
for 0.0333333h;
Yield given;
|
|
|
With
zeolite NaY; bromine;
In
dichloromethane;
at 20 ℃;
for 5h;
|
97 % Chromat. |
|
Multi-step reaction with 2 steps
1: AlCl3 / 45 °C
2: iron-turnings; tetrachloromethane; bromine
With
tetrachloromethane; aluminium trichloride; bromine; iron;
|
|
|
With
N-Bromosuccinimide;
at 20 ℃;
for 16h;
regioselective reaction;
|
bromobenzene
2-methyl-propan-1-ol
tert-butylbenzene
1,4-di-tert-butylbenzene
4-Brom-3-chlormethyl-tert.-butyl-benzol
(4-tert-butylphenyl)trimethylsilane
1-(4-tert-Butyl-phenyl)-2-methyl-2-phenyl-propan-1-ol
1-tert-Butyl-4-(2,2-dimethylpropyl)benzol